A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066411



Internal ID19155630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:62155698..62251211hg38UCSC Ensembl
Innerchr16:62189602..62285115hg19UCSC Ensembl
Innerchr16:60747103..60842616hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3895514
hg1995514
hg1895514
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559370
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066411
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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